Author Archive

The hydrogen evolution

An inexpensive, easy to assemble light-activated water-splitting system for generating hydrogen has been devised by UK scientists.

Erwin Reisner at the University of Manchester* attached an inexpensive metal, cobalt, to ruthenium dye-sensitised titania nanoparticles. They placed the nanoparticles in water, added triethanolamine (which donates an electron), stirred the mixture at room temperature and found that hydrogen was generated.

Nanoparticles show excellent dispersibility in water and the high surface area allows for easy variation of the catalyst loading and ratio for the optimisation of light absorption and catalysis, says Reisner.

Download Reisner’s ChemComm communication to find out more. This article is part of the ChemComm Hydrogen web theme.

*now at the University of Cambridge

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Bacteria-based AND gate: a decision-making and self-powered biosensor

Scientists have made the first Boolean logic gate that is purely bacteria-based. It uses the biochemical networks of whole and living bacteria to perform its biocomputing function.

Various logic gates (i.e. AND, OR, XOR) have been made using enzymatic bioelectrochemical systems (BESs), where enzymatic reactions form the core parts of the gates. But until now, microbial BESs, which have electrochemically active bacteria at the electrodes to catalyse oxidation and reduction reactions, have never been used as logic systems.

Largus Angenent, at Cornell University, Ithaca, US, and colleagues used Pseudomonas aeruginosa mutant bacteria in their AND logic gate. P. aeruginosa is an opportunistic pathogen that infects humans (and other organisms), causing a range of problems including inflammation and sepsis. Angenent claims his bacteria-based AND gate could be used in a self-powered, decision-making biosensor to detect or monitor pathogens such as P. aeruginosa.

Graphical abstract: Bacteria-based AND logic gate: a decision-making and self-powered biosensor

To find out more, download Angenent’s ChemComm communication.

If you have some hot research to report, make the right decision and submit to ChemComm.

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New ChemComm Associate Editor

I am delighted to welcome Professor Michael Krische (University of Texas at Austin, USA) as the new ChemComm North American Associate Editor for Organic Chemistry.

His research focuses on catalytic reaction development with applications in natural product synthesis. A central theme involves the identification of new reactivity patterns, the evolution of related catalytic processes and, ultimately, the development of new synthetic strategies.

Professor Krische’s editorial office is now open for submissions in the area of organic chemistry. We look forward to working with him in his new role.

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Doubt cast on X-ray structure of trapped reactive species

Immobilisation inside a cavity can be a very effective strategy for stabilising reactive species. In fact, earlier this year, a team of French scientists claimed in Science1 to have used this technique to elucidate the solid state crystal structure of 1,3-dimethylcyclobutadiene trapped along with carbon dioxide inside an optimised host.

But, says Henry Rzepa from Imperial College London, UK, this claim should be treated with caution as his calculations suggest that the Science report is incorrect.

Based on his quantum chemical modelling studies, Rzepa proposes that reported crystal structure in fact is not that of 1,3-dimethylcyclobutadiene and carbon dioxide, but more probably that of the precursor used to attempt to generate the pair.

Graphical abstract: Can 1,3-dimethylcyclobutadiene and carbon dioxide co-exist inside a supramolecular cavity?

Find out more about this controversial issue in Rzepa’s ChemComm communication (free to access until 25th January 2011) and let us know what you think by leaving your comments below.

For further discussion, see Crystallographic Confusion in Chemistry Views magazine and Henry Rzepa’s blog.

1. Y.-M. Legrand, A. van der Lee, M. Barboiu, Science 2010, 329, 299-302

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Frozen assets in biobanks

Scientists from Sweden have devised a technique that extracts both DNA and RNA from frozen tissue in a bid to improve large-scale extractions from samples stored in biobanks, which could aid cancer research.

Tobias Sjöblom and colleagues from Uppsala University used magnetic silica beads to target and extract DNA and RNA from tissue samples. Because DNA competes with RNA to attach to the beads, the DNA can be recovered first. ‘The technology fulfils an unmet need, so has a huge potential impact on tissue biobanking,’ says Lucy Mathot from Sjöblom’s team.

High quality DNA and RNA preparations are necessary to study genes responsible for cancer and to identify which cancer medication to use. Researchers prefer to carry out analyses using tissues frozen from fresh because the fragments they can get from these samples are longer and better preserved than with alternative methods. Current column-based techniques for the serial extraction of DNA and RNA are labour-intensive so are not suitable for large scale applications and the automation needs of cancer biobanks.

Reaction sequence

Tissue samples are broken down, magnetic silica beads are added, the beads attach to DNA and RNA and are removed with a magnet

Sjöblom’s team broke down the tissue samples by grinding them with a chaotropic salt solution, which helps to break down the DNA and RNA, and then added the magnetic silica beads. When the beads attached to the DNA, they were able to recover the samples with a magnet. Then they captured the remaining RNA in the same way.

Bert Vogelstein, a cancer researcher at the Johns Hopkins University School of Medicine in the US says: ‘The technique looks like it will be quite useful for preparing precious samples for next-generation sequencing analysis.’

In the future, the team plans to implement the procedure on a robotic platform to enable parallel sample processing.

Jennifer Newton

Interested? Read Sjöblom’s ChemComm communication.

Could your work be an asset to ChemComm? Submit today and make an impact.

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Now available – new article templates

We have introduced slightly revised templates for all our article types. This means that the citation information will be much more visible to readers, both online and in print, so should facilitate wider readership of your work.

Make sure you use the latest templates when submitting your next article.

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Ionic liquid could be used as rocket fuel

A hydrazine-based ionic liquid could be used as rocket fuel, say US scientists.

The combustibility of ionic liquids, a hazard for most applications, has inspired researchers to consider them as possible propellants in rocket fuels. Robin Rogers and his colleagues from The University of Alabama in Tuscaloosa and C3 Propulsion in Huntsville have found that an ionic liquid based on one of the most widely used rocket fuel propellants, hydrazine, ignited on contact with a catalyst, without the need for an oxidant or an ignition source.

The team studied the behaviour of nitrate salts of 2-hydroxyethylhydrazinium upon addition of various catalysts. It was found that in the presence of one particular solid catalyst, Ir-alumina (known as Shell 405), and at temperatures above only 100 °C, the salts ignited, producing smoke and gas.

Addition of 2-hydroxyethylhydrazinium dinitrate to the solid catalyst Shell 405, followed by smoke, flame and residual catalyst

Rogers explains that the impetus for the research was increased safety: ‘we wanted to see if we could take a hydrazine-like molecule, which is volatile, turn it into a non-volatile salt and yet still have the same reactivity that the hydrazine did. We were pretty excited because it worked.’

In addition to decreasing vapour toxicity by replacing hydrazine with an ionic liquid, this material could lead to safer, more efficient, forms of rocket fuel since ignition could occur simply by running the ionic liquid over a catalyst bed, eliminating the need for stabilisers or an additional liquid oxidant.

‘Clearly, this is not only a safer way of propellant ignition, it is also more effective as it allows for low temperature combustion,’ says Christopher Hardacre, an expert in ionic liquids and catalysis from Queen’s University Belfast in Northern Ireland. Hardacre adds that the low volatility associated with ionic liquids as well as the low cost of the materials makes this propellant system even more attractive for various applications.

The work is still in its infancy and the next step will be to optimise the material for specific applications. ‘We need the real rocket scientists out there to weigh in and tell us what needs to be improved or to find better molecules or better salts,’ says Rogers.

Patricia Pantos

For more information, download Rogers’ ChemComm communication.

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Drug delivery by bursting microcapsules

Acid degradable microcapsules that deliver their cargo by bursting in acidic environments have been made by US chemists. The non-toxic capsules could be used to deliver drugs directly to cells, claim Jean Fréchet, at UC Berkeley, and colleagues.

Bursting microcapsules

Download Fréchet’s communication for FREE until 24th December. You might also be interested in a recent J. Mater. Chem. article on a tumour-targeting drug carrier with a pH-controlled release system, which uses graphene oxide as the carrier.

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Versatile variation on the Fischer indole synthesis

UK chemists have developed a new variation on a famous route to indoles that uses more readily available starting materials.

The Fischer reaction involves the functionalisation of an unactivated C-H position by way of a [3,3]-sigmatropic shift. It is simple and convenient – it couples a mono-functionalised arene with a readily available ketone or aldehyde – but is hindered by the lack of availability of aryl hydrazine starting materials.

Instead Christopher Moody and Martyn Inman at the University of Nottingham started from readily available haloarenes. They converted them into a wide range of indoles in just two steps by halogen-magnesium exchange, quenching with di-tert-butyl azodicarboxylate, then reacting with ketones under acidic conditions.

Graphical abstract: A two step route to indoles from haloarenes—a versatile variation on the Fischer indole synthesis

This new variation is simple and versatile, says Moody, making it a highly practical alternative modern protocol for making the fundamentally important indole ring system.

Download the article for free until 24th December and let us know what you think of this new route below.

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5th ChemComm International Symposium

The 5th ChemComm  International Symposium will take place in Japan and China in May 2011. The purpose of RSC journal symposia is to bring together scientists in a stimulating and friendly environment that will foster collaborations between the researchers and the universities involved in the meetings.

The symposium will feature three one-day meetings. Each one day meeting will feature a selection of lectures covering organic chemistry and catalysis given by some of the world’s leading international scientists. The first one-day meeting, will be held at Kyoto University, Japan, before the symposium moves to China for two further events. The second one-day meeting will be held in Lanzhou University with the final instalment taking place at Nankai University, Tianjin. The symposium is organised by Chemical Communications, the Royal Society of Chemistry and the local host organisations.

The symposium will appeal to academic and industrial scientists with an interest in organic chemistry and catalysis. Attendance at the symposium is free of charge and student participation is strongly encouraged.

For more information on the dates, venues and speakers please visit the symposium website.

ChemComm Editor Robert Eagling with his two Korean hosts from the 4th ChemComm symposia

ChemComm Editor Robert Eagling with his two Korean hosts from the 4th ChemComm symposium

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